HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Pyridinecarboxaldehyde → Bis(6-methyl-2-pyridyl) diketone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Pyridinecarboxaldehyde | HCID 14273 | — |
| Reactant | 6-Methyl-2-pyridylmethanol | HCID 70736 | — |
| Reactant | 2-Hydroxy-1,2-bis(6-methyl-2-pyridinyl)ethanone | HCID 97927 | — |
| Reactant | HCID 24763988 | HCID 24763988 | — |
| Product | Bis(6-methyl-2-pyridyl) diketone | HCID 81128 | — |
| Product | HCID 24764031 | HCID 24764031 | — |
Reaction Steps
In addition, in the reaction between 2-pyridinecarboxaldehyde with (6-methylpyridine-2-yl)methanol shown below as reaction 5, the main products obtained are keto-enol compounds: 2-hydroxy-1,2-bis(6-methyl-2-pyridyl)-1-ethanone and 2-hydroxy-1-(6-methyl-2-pyridyl)-2-(2-pyridyl)-1-ethanone. Subsequent treatment with solvent produces 1,2-bis(6-methylpyridine-2-yl)ethane-1,2-dione and 1-(pyridine-2-yl)-2-(6-methylpyridine-2-yl)ethane-1,2-dione and in a much lesser quantity 1,2-bis(6-methylpyridine-2-yl)ethene-1,2-diol (M. J. Percino, V. M. Chapela, O. Urzua, H. Toribio, C. Rodriguez-Barbarin Journal of Chemical Research, (2007), 187).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07989583B2 |
| Source dataset | uspto-grants-2011_08 |
| ORD ID | ord-3b882a22581f4d64b3f2b8f4dd2fb0b1 |
| Source note | uspto-grants-2011_08 |